Brudenell Suzanne J., Spiccia Leone, Bond Alan M., Comba Peter, Hockless David C. R.
Department of Chemistry, Monash University, Clayton, Victoria 3168, Australia, Anorganisch-Chemisches Institut, University of Heidelberg, Im Neuenheimer Feld 270, 69120, Heidelberg, Germany, and Research School of Chemistry, Australian National University, Canberra ACT 2601, Australia.
Inorg Chem. 1998 Jul 27;37(15):3705-3713. doi: 10.1021/ic971634i.
Structural, electrochemical, and EPR studies of binuclear copper(II) complexes of bis(pentadentate) ligands, obtained by attaching 2-pyridylmethyl arms to the four secondary nitrogens of bis(tacn) macrocycles linked by ethyl (tmpdtne, Cu(2)(tmpdtne)(4).2H(2)O 2), propyl (tmpdtnp, Cu(2)(tmpdtnp)(4) 3), butyl (tmpdtnb, Cu(2)(tmpdtnb)(4) 4), m-xylyl (tmpdtnm-X, Cu(2)(tmpdtnm-X)(4).2DMSO.2H(2)O, 5), and 2-propanol (tmpdtnp-OH, Cu(2)(tmpdtnp-OH)(4).2H(2)O, 6) bridges, are reported, together with further analysis of the mononuclear complex, Cu(dmptacn)(2) 1, dmptacn = 1,4-bis(2-pyridylmethyl)-1,4,7-triazacyclononane. Single-crystal X-ray diffraction studies established the molecular structure of 3 and the tetrakis(DMF) solvate of 4. Complex 3 crystallizes in the monoclinic space group P2(1)/c (No. 14) with a = 13.867(3), b = 13.548(6), c = 28.055(4) Å, beta = 102.63(1) degrees, V= 5143(2) Å(3), and Z = 4. Refinement gave R = 0.085 and R(w) = 0.089 for 3696 observed reflections. 4 crystallizes in the triclinic space group &Pmacr; (No. 2) with a = 11.775(4), b = 12.718(3), c = 13.201(3) Å, alpha = 61.25(2), beta = 75.99(3), gamma = 77.66(3) degrees, V = 1673(1) Å(3), and Z = 1. Refinement gave R = 0.072 and R(w) = 0.065 for 3876 observed reflections. In 4, the pentadentate compartments are oriented in an anti configuration, while in 3, constraints introduced by the propane bridging group result in a syn configuration. Both complexes exhibit distorted square pyramidal (SP) geometries about the Cu(II) centers with Cu-N(apical) approximately 2.25 Å and Cu-N(equatorial) approximately 2.0 Å. Molecular mechanics calculations have been carried out on these types of complexes for the first time in order to predict the solution structures of 5 and 6. The calculations revealed that the SP geometry is also preferred by these complexes and that there is little energy difference between the syn and anti configurations. Cyclic, square-wave, and steady-state voltammetric studies on 1-6 indicate that, on the time scale of the measurements, 1 undergoes a one-electron reduction to the Cu(I) state while 2-6 undergo an overall two-electron reduction to the binuclear Cu(I) complexes. For 2-4, a shift in reduction potential to more negative values with increasing Cu.Cu separation reflects the stabilization of the Cu(II) state while the two partially resolved reduction processes for 6 suggest that the alcohol group in the ligand backbone promotes a small level of interaction between copper centers.
